Studies on the total synthesis of (2R, 4'R, 8'R)-.alpha.-tocopherol (vitamin E). Stereospecific cyclizations leading to optically active chromans
- 1 June 1981
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 46 (12) , 2445-2450
- https://doi.org/10.1021/jo00325a004
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- A novel total synthesis of (2R,4'R,8'R)-.alpha.-tocopherol (vitamin E). Construction of chiral chromans from an optically active, nonaromatic precursorJournal of the American Chemical Society, 1979
- Totalsynthese von natürlichem α‐Tocopherol 3. Mitteilung. Aufbau der Seitenkette mit (−)‐(S)‐2‐Methyl‐γ‐butyrolacton als zentralem BausteinHelvetica Chimica Acta, 1979
- Synthetic studies on (2R,4'R,8'R)-.alpha.-tocopherol. Facile syntheses of optically active, saturated, acyclic isoprenoids via stereospecific [3,3] sigmatropic rearrangementsThe Journal of Organic Chemistry, 1976
- Syntheses of (2R, 4′R, 8′R)‐α‐Tocopherol and (2R, 3′E, 7′E)‐α‐TocotrienolHelvetica Chimica Acta, 1976
- Über die Chemie des Vitamins E. 3. Mitteilung. Die Totalsynthese von (2R, 4′R, 8′R)‐ und (2S, 4′R, 8′R)‐α‐TocopherolHelvetica Chimica Acta, 1963